Mutación de novo (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Mutación de novo" in Spanish language version.

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Veltman, Joris A.; Brunner, Han G. (2012). «De novo mutations in human genetic disease». Nature Reviews Genetics 13 (8): 565-575. PMID 22777127. doi:10.1038/nrg3241.
Sanders, Stephan J.; Ercan-Sencicek, Gunes A.; Hus, Varun; Willsey, A. Jeremy; Murtha, Michael T.; Moreno-De-Luca, Daniela; Cho, Judy; Shi, Yunjia (2011). «Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism». Neuron 70 (5): 863-885. PMID 21658581. doi:10.1016/j.neuron.2011.05.002.
Li, Jingjing; Oehlert, John; Snyder, Michael; Stevenson, David K.; Shaw, Gary M. (7 de abril de 2017). «Fetal de novo mutations and preterm birth». PLOS Genetics 13 (4): e1006689. ISSN 1553-7390. PMC 5384656. PMID 28388617. doi:10.1371/journal.pgen.1006689.
Rahbari, R.; Wuster, A.; Lindsay, S.J.; Hurst, J.M.; Rahbari, R. (2016). «Timing, rates and spectra of human germline mutation». Nature Genetics 48 (2): 126-133. PMID 26656846. doi:10.1038/ng.3469.

Li, Jingjing; Oehlert, John; Snyder, Michael; Stevenson, David K.; Shaw, Gary M. (7 de abril de 2017). «Fetal de novo mutations and preterm birth». PLOS Genetics 13 (4): e1006689. ISSN 1553-7390. PMC 5384656. PMID 28388617. doi:10.1371/journal.pgen.1006689.

Veltman, Joris A.; Brunner, Han G. (2012). «De novo mutations in human genetic disease». Nature Reviews Genetics 13 (8): 565-575. PMID 22777127. doi:10.1038/nrg3241.
Sanders, Stephan J.; Ercan-Sencicek, Gunes A.; Hus, Varun; Willsey, A. Jeremy; Murtha, Michael T.; Moreno-De-Luca, Daniela; Cho, Judy; Shi, Yunjia (2011). «Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism». Neuron 70 (5): 863-885. PMID 21658581. doi:10.1016/j.neuron.2011.05.002.
Li, Jingjing; Oehlert, John; Snyder, Michael; Stevenson, David K.; Shaw, Gary M. (7 de abril de 2017). «Fetal de novo mutations and preterm birth». PLOS Genetics 13 (4): e1006689. ISSN 1553-7390. PMC 5384656. PMID 28388617. doi:10.1371/journal.pgen.1006689.
Rahbari, R.; Wuster, A.; Lindsay, S.J.; Hurst, J.M.; Rahbari, R. (2016). «Timing, rates and spectra of human germline mutation». Nature Genetics 48 (2): 126-133. PMID 26656846. doi:10.1038/ng.3469.